Day 35/35 of chemo and radiation.
There were so many reasons to believe that we would never see this day.
The scant amount of data that exists put the odds of him making it this far at 33%.
And by “making it,”
I mean staying alive.
In preparation for these 35 days,
we revised our Health Care Directive,
we crafted our will,
we made no plans beyond April.
That’s how poor the odds were.
When they handed us the schedule of appointments for these 35 days,
I internally rolled my eyes.
Never, in these eight years of medical madness,
has a long term schedule mapping out how things will go,
been seen to the end.
His body always has a way of throwing a wrench into the plans,
doing the things that no one expects,
the quirks found only in fine print, under,
”In rare situations….”
Each of the 35 days,
I witnessed the effects of treatment on an elderly woman at the radiation suite.
I watched the progression as
at first she walked in to her appointments,
then began to be pushed in a wheelchair by her family members,
then saw evidence that she had been hospitalized, as she was pushed in a wheelchair by hospital transport,
and then wheeled in via hospital bed for treatments, tubes and wires attached to all the places,
a daily cataloging of decline.
I assumed her trajectory would be ours,
that she was our crystal ball
showing us what was to come.
I thought that IF he was able to get through all 35,
(and that IF felt large and looming),
that certainly the last few weeks would be spent
in the hospital,
that for the final treatments
he would be wheeled in via hospital bed, tubes and wires attached to all the places.
I would have
that on day 35
we would be leaving from our OWN HOUSE to drive to the hospital for treatment.
But drive we did,
his brother in tow,
marrow donor and best friend,
there to witness this milestone
as he has so many others.
When we arrived at the hospital and I asked if he needed a wheelchair,
on his own two feet
from the car
from our own house
to his last day of treatment,
When we got to the radiation suite,
we were greeted by
our American Cancer Society advocate turned friend,
all ready to celebrate this incredible day.
The six of us family members
tromped back together to the treatment room,
our daughter’s eyes wide as she took in the machine that had been radiating her dad these past 34 days.
We watched as he gave them his birthdate, one last time.
We watched as they handed him his mouthpiece, one last time.
We watched as they snapped the mask on to his face and neck, one last time.
We watched as they covered him with a warm blanket,
one last time.
And then we all left the room,
leaving the machine to do its thing,
to have one last shot at eradicating any bits of cancer that may still remain.
All of us,
even the techs,
had to exit the room
for fear of the damage the machine would do to us if we stayed,
damage that had purposely been done to my beloved
When he emerged
just ten minutes later,
the celebration began.
Every one who worked with him over these 35 days
each one having played an integral part in these 35 days,
was present as he
RANG THE BELL,
the bell that signifies the end of treatment,
the bell I wasn’t sure he’d ever ring,
let alone ring standing there,
on his own two feet,
not a current patient in the hospital.
Everyone present knew this moment was
and handled the enormity of that in their own way:
our pre-teen daughter by scowling,
the receptionist by weeping,
the doctor by blushing, blinking wet eyes, and mumbling, “See you for follow-up on Monday.”
The world is a different place
after the successful completion of these 35 treatments.
His survival changes the narrative and potential treatment plans around radiation and chemo in Fanconi anemia patients.
The next person may not have to hear and feel the helplessness related to the phrase, “We are in a data-free zone.”
The staff who cared for him these 35 days, came to fully recognize that what makes him rare goes way beyond his diagnosis.
They saw and experienced in him a man who, even on his most miserable days, took time and energy to make them laugh, ask how they were,
to care for them as much if not more than they cared for him.
Our family has changed in these 35 days.
We feel we have been given a gift.
We did not assume that we would be a family of three by day 35,
yet here we are.
We battled these 35 days together,
never assuming things would go our way,
but fighting through each day nonetheless,
determined that if things didn’t go well it would be because of DNA breakdown,
not because we’d given up.
We know that the radiation effects will worsen in the weeks to come.
We know that it’s possible that these 35 treatments did not fully demolish the cancer in his throat.
We know that this cancer will not be his last.
But we also know that we just beat the odds
by making it through
of chemo and radiation,
and for today,
that feels like everything.
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